Luminescent tetradentate ligand-containing gold(iii) compounds for organic light-emitting devices and their preparation

ABSTRACT

A series of thermally stable and highly luminescent cyclometalated tetradentate ligand-containing gold(III) compounds was designed and synthesized. The cyclometalated tetradentate ligand-containing gold(III) compounds can be used as light-emitting material for fabrication of light-emitting devices. The cyclometalated tetradentate ligand-containing gold(III) compounds can be deposited as a layer or a component of a layer using a solution-processing technique or a vacuum deposition process. The cyclometalated tetradentate ligand-containing gold(III) compounds are robust and can provide electroluminescence with high efficiency and brightness. More importantly, the vacuum-deposited OLEDs demonstrate long operational stabilities with half-lifetime of over 29,700 hours at 100 cd m −2 .

RELATED APPLICATIONS

This application claims priority to provisional application Ser. No.62/783,829 filed Dec. 21, 2018 which is incorporated by reference in itsentirety.

1. FIELD

Described herein are luminescent cyclometalated tetradentateligand-containing gold(III) compounds and the syntheses of thesecompounds. These compounds can be used as light-emitting materials inphosphorescent organic light-emitting devices (PHOLEDs). In specificembodiments, the compounds have good operational stability withhalf-lifetime over 29,700 hours at 100 cd m⁻².

2. BACKGROUND

Taking the advantages of low cost, light weight, low power consumption,high brightness, excellent color tunability, wide viewing angle of up to180 degrees as well as their ease of fabrication onto flexiblesubstrates, organic light-emitting devices (OLEDs) are considered asremarkably attractive candidates for flat panel displays and solid-statelighting systems. Compared with the pure organic counterparts,transition metal complexes have been extensively studied over the pastthree decades due to the presence of the heavy metal center, which caneffectively lead to a strong spin-orbit coupling and thus promotes anefficient intersystem crossing to harvest triplet excitons forgenerating phosphorescence. This can theoretically result in a four-foldenhancement in the internal quantum efficiency (IQE) of the OLEDs up to100% due to the harvesting of all triplet and singlet excitons.Typically, an OLED consists of several layers of semiconductorssandwiched between two electrodes. The cathode is composed of a low workfunction metal or metal alloy deposited by vacuum evaporation, whereasthe anode is a transparent conductor such as indium tin oxide (ITO).Upon the application of a DC voltage, holes injected by the ITO anodeand electrons injected by the metal cathode will recombine to formexcitons. Subsequent relaxation of excitons will then result in thegeneration of electroluminescence (EL).

The EL from organic materials was first discovered in anthracenecrystals immersed in liquid electrolyte in 1965 [Helfruch, W.;Schneider. W. G. Phys. Rev. Lett. 14, 229 (1965)]. Although a loweroperating voltage could be achieved by using a thin film of anthracenewith solid electrodes, very low efficiencies were encountered with thesesingle-layer devices. Meanwhile, EL from organic polymers was initiallyreported in the 1970s [Kaneto, K.; Yoshino, K.; Koa, K.; Inuishi, Y.Jpn. J. Appl. Phys. 13, 1023 (1974)], where green emission frompolyethylene terephthalate was observed when an impulse voltage wasapplied. The breakthroughs that led to the exponential growth of thisfield and to its first commercialized products can be traced to twosuccessful demonstrations. Tang and VanSlyke proposed the use of adouble-layer structure of vacuum deposited, small-molecular films, inwhich tris(8-hydroxyquinoline)aluminum (Alq₃) was utilized both aslight-emitting layer and electron transporting layer [Tang, C. W.;VanSlyke, S. A. Appl. Phys. Lett. 51, 913 (1987)]. Later, the firstpolymeric light-emitting device was developed by Burroughs et al. in1990 [Burroughs, J. H.; Bradley, D. D. C.; Brown, A. R.; Marks, N.;Friend, R. H.; Burn, P. L.; Holmes, A. B. Nature 347, 539 (1990)], inwhich a yellow-green EL from poly(p-phenylenenvinylene) (PPV) wasachieved. Since then, a number of new electroluminescent small molecularand polymeric light-emitting materials have been investigated withimproved light-emitting properties. The key advantage of using polymersas light-emitting materials is their high solubility in most of thecommon organic solvents, and thus OLEDs can be easily fabricated byusing low-cost and efficient wet processing techniques, such asspin-coating, screen-printing, or ink-jet printing [Burrows, P. E.;Forrest, S. R.; Thompson, M. E. Curr. Opin. Solid State Mat. Sci. 2, 236(1997)].

In 1998, Baldo et al. demonstrated an efficient PHOLED with high IQE byusing platinum(II) 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin(PtOEP) as a dopant [Baldo, M. A.; O′Brien, D. F.; You, Y.; Shoustikow,A.; Sibley, S.; Thompson, M. E.; Forrest, S. R. Nature 395, 151 (1998);O'Brien, D. F.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. Appl.Phys. Lett. 74, 442 (1999)]. Such multilayer device consisted of anemitting layer of Alq₃ doped with PtOEP and showed a strong emission at650 nm arising from the triplet excitons of PtOEP. Since then, a largenumber of metal complexes have been demonstrated with excellentphotophysical properties. Particularly, cyclometalated iridium(III)compounds are one of the most widely investigated classes of metalcomplexes. Most of the cyclometalated iridium(III) complexes showintense phosphorescence and have been extensively investigated for thefabrication of high efficiency OLEDs. Of particular interest is thedevelopment of iridium(III) complexes with 2-phenylpyridine ligand(s).In 1999, Thompson, Forrest and co-workers have demonstrated moreefficient PHOLEDs based on fac-tris(2-phenylpyridine)iridium(III)[Ir(ppy)₃] as phosphorescent emitting material doped in a4,4′-N,N′-dicarbazole-biphenyl (CBP) host [Baldo, M. A.; Lamansky, S.;Burrows, P. E.; Thompson. M. E.; Forrest, S. R. Appl. Phys. Lett. 75, 4(1999)]. Another successful iridium(III) complex is sky-blue-emittingiridium(III) bis[2-(4′,6′-difluorophenyl)pyridinato-N,C²]-picolinate[FIr(pic)], which exhibits a higher photoluminescence quantum yield(PLQY) of about 60% in solution and nearly 100% in a solid-state thinfilm when doped into a high triplet energy host [Rausch, A. F.;Thompson, M. E.; Yersin, H. Inorg. Chem. 48, 1928 (2009); Adachi, C;Kwong, R. C.; Djurovich, P. I.; Adamovich, V.; Baldo, M. A.; Thompson,M. E.; Forrest, S. R. Appl. Phys. Lett. 79, 2082 (2001); Kawamura, Y;Goushi, K.; Brooks, J.; Brown, J. J.; Sasabe, H.; Adachi, C. Appl. Phys.Lett. 86, 071104 (2005)]. Highly efficient OLEDs with external quantumefficiencies (EQEs) of up to 30% have recently been demonstrated basedon the iridium(III) systems [Kim, S.-Y; Jeong, W.-I.; Mayr, C.; Park,Y.-S.; Kim, K.-H.; Lee, J.-H.; Moon, C.-K.; Brutting, W.; Kim, J.-J.Adv. Funct. Mater. 23, 3829 (2013); Udagawa, K.; Sasabe, H.; Igarashi,F.; Kido, J. Adv. Opt. Mater. 4, 86 (2015)].

Apart from the iridium(III) systems with d⁶ electronic configuration andoctahedral geometry, the coordination-unsaturated nature of d⁸transition metal complexes with square-planar structures has been foundto provide intriguing spectroscopic and luminescence properties relatedto the unique tendency of these metal centers to exhibit non-covalentmetal metal interactions. Of particular interest is the platinum(II)compounds due to their rich luminescence properties, associated withtheir strong propensity to from Pt . . . Pt and π-π interactions.Notably, unlike the case of the iridium(III) systems, the use ofbidentate cyclometalated ligands will not lead to isomerization duringsynthesis or sublimation. Moreover, further stabilization of theseplatinum(II) complexes can be accomplished through the use of tridentateand tetradentate ligands to give highly robust metal complex systems. Todate, highly efficient OLEDs with power efficiencies of up to 126 lm W⁻¹and EQEs of up to 26.5% have been achieved [Cheng, G.; Kui, S. C.-F.;Ang, W.-H.; Ko, M.-Y; Chow, P.-K.; Kwong, C.-L.; Kwok, C.-C.; Ma, C.;Guan, X.; Low, K.-H.; Su, S.-J.; Che, C.-M. Chem. Sci. 5, 4819 (2014)].In contrast to the isoelectronic platinum(II) compounds, luminescentgold(III) complexes are relatively less explored, probably due to thepresence of low-energy d-d ligand field (LF) states and theelectrophilicity of the gold(III) metal center. It is difficult tocoordinate cyclometalated tetradentate ligands to the gold(III) metalcenter through successive C—H activations, unlike the case for theisoelectronic platinum(II) complexes where cyclometalated tetradentateligands can be easily incorporated into the platinum(II) center viaone-pot reaction. Thus, there is a need to provide gold(III) complexesthat have more enhanced photophysical properties and involve less stepsduring synthesis.

3. SUMMARY

The present disclosure provides a luminescent gold(III) compound havingthe chemical structure shown in the generic formula (I):

wherein:

-   -   (a) Z is selected from the group consisting of B, C, N, O, Si,        P, P(═O), S and Se;    -   (b) rings A and B are each coordinated to the Au atom through a        carbon atom, and are each independently a substituted or        unsubstituted aryl group, preferably a phenyl group, or a        substituted or unsubstituted heteroaryl group;    -   (c) ring C is coordinated to the Au atom through a nitrogen        atom, and is selected from the group consisting of a substituted        or unsubstituted pyridyl group, a substituted or unsubstituted        quinolinyl group, a substituted or unsubstituted isoquinolinyl        group, a substituted or unsubstituted pyrazinyl group, a        substituted or unsubstituted pyrimidinyl group, a substituted or        unsubstituted pyridazinyl group, a substituted or unsubstituted        triazinyl group, a substituted or unsubstituted carbolinyl        group, a substituted or unsubstituted imidazolyl group, a        substituted or unsubstituted benzimidazolyl group, a substituted        or unsubstituted pyrazolyl group, a substituted or unsubstituted        thienopyridinyl, a substituted or unsubstituted furopyridinyl        group, a substituted or unsubstituted selenophenopyridinyl        group, a substituted or unsubstituted thiazolyl group, a        substituted or unsubstituted thiadiazolyl group, a substituted        or unsubstituted oxadiazolyl group, a substituted or        unsubstituted triazolyl group, a substituted or unsubstituted        oxazolyl group and a substituted or unsubstituted isoxazolyl        group,    -   (d) each D is independently at each occurrence absent or a        cyclic or acyclic moiety wherein:        -   the cyclic moiety is selected from the group consisting of a            substituted or unsubstituted aryl group, preferably a phenyl            group, a substituted or unsubstituted heteroaryl group,            preferably a pyridyl group, a substituted or unsubstituted            cycloalkyl group, and a substituted or unsubstituted            polycyclic group; and        -   the acyclic moiety is selected from the group consisting of            a substituted or unsubstituted alkynyl, a substituted or            unsubstituted arylalkynyl, a substituted or unsubstituted            alkyl, a substituted or unsubstituted alkylaryl, a            substituted or unsubstituted alkoxy, a substituted or            unsubstituted arylalkoxy, a substituted or unsubstituted            acene, and a substituted or unsubstituted a heteroacene;    -   (e) E is absent, an acyclic moiety selected from the group        consisting of a substituted or unsubstituted alkynyl, a        substituted or unsubstituted arylalkynyl, a substituted or        unsubstituted alkyl, a substituted or unsubstituted alkylaryl, a        substituted or unsubstituted alkoxy, a substituted or        unsubstituted arylalkoxy, a substituted or unsubstituted        thiolate, a substituted or unsubstituted arylthiolate, a        substituted or unsubstituted phosphide, a substituted or        unsubstituted arylphosphide, a substituted or unsubstituted        boride, a substituted or unsubstituted arylboride, a substituted        or unsubstituted acene and a substituted or unsubstituted        heteroacene,        -   or E, together with Z and the atoms to which they are            respectfully attached forms a cyclic moiety selected from            the group consisting of a substituted or unsubstituted            pyridyl group, a substituted or unsubstituted pyrrolyl            group, a substituted or unsubstituted thiophenyl group, a            substituted or unsubstituted furanyl group, a substituted or            unsubstituted pyrazolyl group, a substituted or            unsubstituted oxazolyl group, a substituted or unsubstituted            imidazolyl group, a substituted or unsubstituted pyrazinyl            group, a substituted or unsubstituted pyrimidinyl group, a            substituted or unsubstituted pyridazinyl group, a            substituted or unsubstituted piperazinyl group, a            substituted or unsubstituted oxazinyl group, a substituted            or unsubstituted morpholinyl group, a substituted or            unsubstituted thiomorpholinyl group, a substituted or            unsubstituted thiazinyl group, and a substituted or            unsubstituted piperidinyl group;        -   or D, E and Z together represent a substituted or            unsubstituted, monocyclic or fused polycyclic aryl or            heteroaryl group;    -   (f) or D, Y and C, and/or D, Y and B, together represent a        substituted or unsubstituted, monocyclic or fused polycyclic        aryl or heteroaryl group;X and Y are each independently at each        occurrence non-coordination sites selected from the group        consisting of, —CRR′, —C═O, —NR, —O, —PR, —P(═O)R, —BR, S, —SO,        —SO₂, —SiRR′, Se, —AsR, —CH═CH— and —CR═CR—′, wherein R and R′        are independently selected from the group consisting of        hydrogen, halogen, aryl, alkyl, heteroaryl, nitro,        trifluoromethyl, cyano, arylether, alkylether, heteroaryl ether,        diarylamine, dialkylamine, diheteroarylamine, diarylborane,        triarylsilane, trialkylsiliane, alkenyl, alkylaryl, cycloalkyl,        haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino,        alkoxy, azo, benzyl, carbonateester, carboxylate, carboxyl,        ketamine, isocyanate, isocyanide, isothiocyanate, nitrile,        nitro, nitroso, phosphine, phosphate, phosphono, pyridyl,        sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted        aryl, heteroaryl, substituted heteroaryl, a heterocyclic group        and derivatives thereof;    -   (g) wherein p, q, r and s are each independently 0, 1, 2 or 3;        and    -   (h) n is zero, a positive integer or a negative integer.    -   It is apparent to a person of skill in the art that n represents        a charge of the complex and is zero (i.e., neutral complex), a        positive integer (i.e., positively charged complex) or a        negative integer (i.e., negatively charged complex).

In certain embodiments, the gold(III) compound is deposited as a thinlayer on a substrate layer. In certain embodiments, the gold(III)compound comprises a thin layer that is prepared by vacuum deposition,spin-coating, or inkjet printing.

In certain embodiments, the gold(III) compound has photoluminescenceproperties within a range of about 380 to 1050 nm.

In certain embodiments, the gold(III) compound emits light in responseto the passage of an electric current or to a strong electric field.

In certain embodiments, the gold(III) compound is used to fabricate anOLED.

In certain embodiments, the gold(III) compound serves as thelight-emitting layer of the OLED.

In certain embodiments, the gold(III) compound serves as a dopant in thelight-emitting layer or emissive layer of the OLED.

Disclosed herein is a method for preparing a luminescent compound withcyclometalated tetradentate ligand comprising the following reaction:

-   -   wherein:    -   (a) G and K are each independently C or N, with G and K are not        the same;    -   (b) R¹, R², R³, R⁴ and R⁵ groups are each independently selected        from the group consisting of OR, NR₂, SR, C(O)R, C(O)OR,        C(O)NR₂, CN, CF3, NO₂, SO₂, SOR, SO₂R, SO₃R, halo, or alkyl,        alkenyl, alkynyl, alkylaryl, aryl and cycloalkyl with one or        more alkyl, alkenyl, alkynyl, alkylaryl, aryl and cycloalkyl        being optionally substituted with one or more OR, NR₂, SR,        C(O)R, C(O)OR, C(O)NR₂, CN, CF₃, NO₂, SO₂, SOR, SO₂R, SO₃R,        halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl        or a heterocyclic group, wherein R is independently at each        occurrence alkyl, alkynyl, alkylaryl, aryl or cycloalkyl; and    -   (c) n is zero, a positive integer or a negative integer.

In certain embodiments, a luminescent compound is prepared.

In certain embodiments, the gold(III) metal center comprises alight-emitting layer of a light-emitting device.

In certain embodiments, the gold(III) metal group comprises a layer of alight-emitting device.

In certain embodiments, the gold(III) metal compound is a dopantincluded in the light-emitting layer or emissive layer of thelight-emitting device.

In certain embodiments, the gold(III) metal compound is a dopantincluded in a light-emitting device.

Provided in this disclosure is a light-emitting device with an orderedstructure comprising an anode, a hole-transporting layer, alight-emitting layer, an electron-transporting layer and a cathodewherein the light-emitting layer comprises a gold(III) compound having achemical structure represented by the following general formula (I),

wherein:

-   -   (a) Z is selected from the group consisting of B, C, N, O, Si,        P, P(═O), S and Se;    -   (b) rings A and B are each coordinated to the Au atom through a        carbon atom, and are each independently a substituted or        unsubstituted aryl group, preferably a phenyl group, or a        substituted or unsubstituted heteroaryl group;    -   (c) ring C is coordinated to the Au atom through a nitrogen        atom, and is selected from the group consisting of a substituted        or unsubstituted pyridyl group, a substituted or unsubstituted        quinolinyl group, a substituted or unsubstituted isoquinolinyl        group, a substituted or unsubstituted pyrazinyl group, a        substituted or unsubstituted pyrimidinyl group, a substituted or        unsubstituted pyridazinyl group, a substituted or unsubstituted        triazinyl group, a substituted or unsubstituted carbolinyl        group, a substituted or unsubstituted imidazolyl group, a        substituted or unsubstituted benzimidazolyl group, a substituted        or unsubstituted pyrazolyl group, a substituted or unsubstituted        thienopyridinyl, a substituted or unsubstituted furopyridinyl        group, a substituted or unsubstituted selenophenopyridinyl        group, a substituted or unsubstituted thiazolyl group, a        substituted or unsubstituted thiadiazolyl group, a substituted        or unsubstituted oxadiazolyl group, a substituted or        unsubstituted triazolyl group, a substituted or unsubstituted        oxazolyl group and a substituted or unsubstituted isoxazolyl        group,    -   (d) each D is independently at each occurrence absent or a        cyclic or acyclic moiety wherein:        -   the cyclic moiety is selected from the group consisting of a            substituted or unsubstituted aryl group, preferably a phenyl            group, a substituted or unsubstituted heteroaryl group,            preferably a pyridyl group, a substituted or unsubstituted            cycloalkyl group, and a substituted or unsubstituted            polycyclic group; and        -   the acyclic moiety is selected from the group consisting of            a substituted or unsubstituted alkynyl, a substituted or            unsubstituted arylalkynyl, a substituted or unsubstituted            alkyl, a substituted or unsubstituted alkylaryl, a            substituted or unsubstituted alkoxy, a substituted or            unsubstituted arylalkoxy, a substituted or unsubstituted            acene, and a substituted or unsubstituted a heteroacene;    -   (e) E is absent, an acyclic moiety selected from the group        consisting of a substituted or unsubstituted alkynyl, a        substituted or unsubstituted arylalkynyl, a substituted or        unsubstituted alkyl, a substituted or unsubstituted alkylaryl, a        substituted or unsubstituted alkoxy, a substituted or        unsubstituted arylalkoxy, a substituted or unsubstituted        thiolate, a substituted or unsubstituted arylthiolate, a        substituted or unsubstituted phosphide, a substituted or        unsubstituted arylphosphide, a substituted or unsubstituted        boride, a substituted or unsubstituted arylboride, a substituted        or unsubstituted acene and a substituted or unsubstituted        heteroacene,        -   or E, together with Z and the atoms to which they are            respectfully attached forms a cyclic moiety selected from            the group consisting of a substituted or unsubstituted            pyridyl group, a substituted or unsubstituted pyrrolyl            group, a substituted or unsubstituted thiophenyl group, a            substituted or unsubstituted furanyl group, a substituted or            unsubstituted pyrazolyl group, a substituted or            unsubstituted oxazolyl group, a substituted or unsubstituted            imidazolyl group, a substituted or unsubstituted pyrazinyl            group, a substituted or unsubstituted pyrimidinyl group, a            substituted or unsubstituted pyridazinyl group, a            substituted or unsubstituted piperazinyl group, a            substituted or unsubstituted oxazinyl group, a substituted            or unsubstituted morpholinyl group, a substituted or            unsubstituted thiomorpholinyl group, a substituted or            unsubstituted thiazinyl group, and a substituted or            unsubstituted piperidinyl group;        -   or D, E and Z together represent a substituted or            unsubstituted, monocyclic or fused polycyclic aryl or            heteroaryl group;    -   (f) or D, Y and C, and/or D, Y and B, together represent a        substituted or unsubstituted, monocyclic or fused polycyclic        aryl or heteroaryl group;X and Y are each independently at each        occurrence non-coordination sites selected from the group        consisting of, —CRR′, —C═O, —NR, —O, —PR, —P(═O)R, —BR, S, —SO,        —SO₂, —SiRR′, Se, —AsR, —CH═CH— and —CR═CR—′, wherein R and R′        are independently selected from the group consisting of        hydrogen, halogen, aryl, alkyl, heteroaryl, nitro,        trifluoromethyl, cyano, arylether, alkylether, heteroaryl ether,        diarylamine, dialkylamine, diheteroarylamine, diarylborane,        triarylsilane, trialkylsiliane, alkenyl, alkylaryl, cycloalkyl,        haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino,        alkoxy, azo, benzyl, carbonateester, carboxylate, carboxyl,        ketamine, isocyanate, isocyanide, isothiocyanate, nitrile,        nitro, nitroso, phosphine, phosphate, phosphono, pyridyl,        sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted        aryl, heteroaryl, substituted heteroaryl, a heterocyclic group        and derivatives thereof;    -   (g) wherein p, q, r and s are each independently 0, 1, 2 or 3;        and    -   (h) n is zero, a positive integer or a negative integer.

In certain embodiments, the light-emitting layer or emissive layer isprepared using vacuum deposition or solution processing technique.

Provided in this disclosure is an apparatus comprising: a compounddisclosed herein, wherein the apparatus is selected from the groupconsisting of a television, a copier, a printer, a liquid crystaldisplay, a measuring instrument, a display board, a marker lamp, anelectrophotographic photoreceptor, a photoelectric transducer, a solarcell or an image sensor, such that the apparatus incorporates thecompound for light emission purposes.

In one or more embodiments, a new class of gold(III) complexes withtetradentate ligands that can be obtained from a simple one-pot reactionis provided. Particularly, the claimed compounds can be prepared bySuzuki-Miyaura cross-coupling followed by Buchwald-Hartwigcross-coupling of the gold(III) precursor complex and the precursorligand, with intramolecular cyclization occurring spontaneously togenerate the gold(III) complexes with tetradentate ligands in one pot.This can significantly increase the ease of preparation and reduction inthe number of steps for synthesis and purification, as well as improvethe product yield. This will no doubt be of great benefit to display andsolid-state lighting companies. The more rigid tetradentate ligandframework can effectively rigidify the molecule and reduce thenon-radiative decay, and thus improve the chemical and thermalstabilities of the claimed gold(III) complexes, as exemplified by theirhigh decomposition temperatures of 350-500° C. In addition, the emissioncolor of the tetradentate gold(III) complexes can be effectively tunedby changing the N-donor atoms on the cyclometalating tetradentateligand. This opens up a possibility to fabricate the devices by eithervacuum deposition or solution-processing techniques, such asspin-coating and ink-jet printing. High performance vacuum-deposited andsolution-processable OLEDs with EQEs of 5-30% and 2-20%, respectively,have been demonstrated. More importantly, such vacuum-deposited devicesshow satisfactory long operational stabilities with half-lifetime of5000-30,000 hours at 100 cd m⁻².

4. BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed incolor. Copies of this patent or patent application publication withcolor drawings will be provided by the Office upon request and paymentof the necessary fee.

The disclosure is illustrated in the figures of the accompanyingdrawings which are meant to be exemplary and not limiting, in which likereferences are intended to refer to like or corresponding parts, and inwhich:

FIG. 1 is a schematic diagram of the basic structure of an organic ELdevice, in accordance with one or more embodiments herein.

FIG. 2 shows the UV-visible absorption spectra of compounds 1, 3 and 4in toluene at 298 K, in accordance with one or more embodiments herein.

FIG. 3 shows the normalized photoluminescence (PL) spectra of compounds1, 3 and 4 in toluene at 298 K, in accordance with one or moreembodiments herein.

FIG. 4 shows the normalized PL spectra of thin films of compounds 1, 3,4 and 7 doped into 1,3-bis(carbazol-9-yl)benzene (MCP) at 10 wt % at 298K, in accordance with one or more embodiments herein.

FIG. 5 shows the solid-state thin film emission spectra of compound 1doped into MCP at 5, 10, 15 and 20 wt % at 298 K, in accordance with oneor more embodiments herein.

FIG. 6 shows the thermogravimetric analysis (TGA) trace of compound 1,in accordance with one or more embodiments herein.

FIG. 7 shows the TGA trace of compound 2, in accordance with one or moreembodiments herein.

FIG. 8 shows the TGA trace of compound 3, in accordance with one or moreembodiments herein.

FIG. 9 shows the TGA trace of compound 4, in accordance with one or moreembodiments herein.

FIG. 10 shows the normalized EL spectra of the solution-processabledevices made with compound 1.

FIG. 11 shows the EQEs of the solution-processable devices made withcompound 1.

FIG. 12 shows the normalized EL spectra of the solution-processabledevices made with compound 3.

FIG. 13 shows the EQEs of the solution-processable devices made withcompound 3.

FIG. 14 shows the normalized EL spectra of the solution-processabledevices made with compound 4.

FIG. 15 shows the EQEs of the solution-processable devices made withcompound 4.

FIG. 16 shows the EQEs of the vacuum-deposited devices made withcompound 1.

FIG. 17 shows the EQEs of the vacuum-deposited devices made withcompound 2.

FIG. 18 shows the EQEs of the vacuum-deposited devices made withcompound 3.

FIG. 19 shows the EQEs of the vacuum-deposited devices made withcompound 4.

FIG. 20 shows the relative luminance of devices made with compounds 1and 4 as a function of time.

FIG. 21 shows the angular-dependent PL intensities of p-polarized lightof 1, 3 and 4 doped into 3,3′-di(9H-carbazol-9-yl)-1,1′-biphenyl (m-CBP)thin films.

FIG. 22 shows the two-dimensional distribution of the emission spectravs. the angle of the m-CBP thin films doped with 1, 3 and 4.

DETAILED DESCRIPTION 4.1. Definitions

In the present disclosure the following terms are used.

The term “halo” or “halogen” or “halide” as used herein includesfluorine, chlorine, bromine and iodine.

The term “pseudohalide” as used herein includes, but are not limited to,cyanate, thiocyanate and cyanide.

The term “alkyl” as used herein includes straight and branched chainalkyl groups. Preferred alkyl groups are those containing between one toeighteen carbon atoms and includes methyl, ethyl, propyl, isopropyl,butyl, isobutyl, tert-butyl, and other similar compounds. In addition,the alkyl group may be optionally substituted with one or moresubstituents selected from the group consisting of hydrogen atom,deuterium atom, formaldehyde, cyano, alkylalkynyl, substitutedalkylalkynyl, arylalkynyl, substituted arylalkynyl, heteroarylalkynyl,substituted heteroarylalkynyl, condensed polycyclic, substitutedcondensed polycyclic, aryl, alkyl, heteroaryl, nitro, trifluoromethane,cyano, arylether, alkylether, heteroarylether, diarylamine,dialkylamine, diheteroarylamine, diarylborane, triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl, haloformyl, hydroxyl,aldehyde, carboxamide, amine, amino, alkoxy, azo, benzyl, carbonateester, carboxylate, carboxyl, ketamine, isocyanate, isocyanide,isothiocyanate, nitrile, nitro, nitroso, phosphine, phosphate,phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl,substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic andderivatives thereof.

The term “alkenyl” as used herein includes both straight and branchedchain alkene radicals.

Preferred alkenyl groups are those containing between two and eighteencarbon atoms. In addition, the alkenyl group may be optionallysubstituted with one or more substituents including alkyl, alkenyl,alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano, alkylalkynyl,substituted alkylalkynyl, arylalkynyl, substituted arylalkynyl,heteroarylalkynyl, substituted heteroarylalkynyl, condensed polycyclic,substituted condensed polycyclic, aryl, alkyl, heteroaryl, nitro,trifluoromethane, aryl ether, alkylether, heteroarylether, diarylamine,dialkylamine, diheteroarylamine, diarylborane, triarylsilane,trialkylsilane, alkenyl, alkylaryl, cycloalkyl, haloformyl, hydroxyl,aldehyde, carboxamide, amine, amino, alkoxy, azo, benzyl, carbonateester, carboxylate, carboxyl, ketamine, isocyanate, isocyanide,isothiocyanate, nitrile, nitro, nitroso, phosphine, phosphate,phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl,substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic,NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ and derivatives thereof;and R and R′ are independently selected from the group consisting ofhydrogen atom, deuterium atom, formaldehyde, cyano, alkylalkynyl,substituted alkylalkynyl, arylalkynyl, substituted arylalkynyl,heteroarylalkynyl, substituted heteroarylalkynyl, condensed polycyclic,substituted condensed polycyclic, aryl, alkyl, heteroaryl, nitro,trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkynyl” as used herein includes both straight and branchedchain alkyne radicals. Preferred alkynyl groups are those containingbetween two and eighteen carbon atoms. In addition, the alkynyl groupmay be optionally substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkylaryl” as used herein includes an aryl group which has analkyl group as a substituent. In addition, the alkylaryl group may beoptionally substituted with one or more substituents including alkyl,alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkenylaryl” as used herein includes an aryl group which hasan alkenyl group as a substituent. In addition, the alkenylaryl groupmay be optionally substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkynylaryl” as used herein includes an aryl group which hasan alkynyl group as a substituent. In addition, the alkynylaryl groupmay be optionally substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkylalkenyl” as used herein includes an alkenyl group whichhas an alkynyl group as a substituent. In addition, the alkylalkenylgroup may be optionally substituted with one or more substituentsincluding alkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde,cyano, alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “arylalkenyl” as used herein includes an alkenyl group has anaryl group as a substituent. In addition, the arylalkenyl group may beoptionally substituted with one or more substituents including alkyl,alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkynylalkenyl” as used herein includes an alkenyl group whichhas an alkynyl group as a substituent. In addition, the alkynylalkenylgroup may be optionally substituted with one or more substituentsincluding alkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde,cyano, alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkylalkynyl” as used herein includes an alkynyl group whichhas an alkyl group as a substituent. In addition, the alkylalkynyl groupmay be optionally substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “arylalkynyl” as used herein includes an alkynyl group whichhas an aryl group as a substituent. In addition, the arylalkynyl groupmay be optionally substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “cycloalkyl” as used herein includes cyclic alkylgroups.Cycloalkyl groups can contain 3 to 7 or more carbon atoms and includescyclopropyl, cyclopentyl, cyclohexyl, and the like. Cycloalkyl group canbe unsubstituted or substituted with one or more substituents includingalkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, aryl ether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR, SOR, SOR, BRR″ andderivatives thereof; and R and R′ are independently selected from thegroup consisting of hydrogen atom, deuterium atom, formaldehyde, cyano,alkylalkynyl, substituted alkylalkynyl, arylalkynyl, substitutedarylalkynyl, heteroarylalkynyl, substituted heteroarylalkynyl, condensedpolycyclic, substituted condensed polycyclic, aryl, alkyl, heteroaryl,nitro, trifluoromethane, cyano, arylether, alkylether, heteroarylether,diarylamine, dialkylamine, diheteroarylamine, diarylborane,triarylsilane, trialkylsilane, alkenyl, alkylaryl, cycloalkyl,haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino, alkoxy, azo,benzyl, carbonate ester, carboxylate, carboxyl, ketamine, isocyanate,isocyanide, isothiocyanate, nitrile, nitro, nitroso, phosphine,phosphate, phosphono, pyridyl, sulfonyl, sulfo, sulfinyl, sulfhydryl,halo, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic and derivatives thereof.

The term “alkoxy” or “alkyloxy” as used herein interchangeably includeslinear or branched alkyl group of 1 to 18 or more carbon atoms bonded toan oxy (0) group, and unsubstituted or substituted with one or moresubstituents including alkyl, alkenyl, alkynyl, alkylaryl, cycloalkyl,formaldehyde, cyano, alkylalkynyl, substituted alkylalkynyl,arylalkynyl, substituted arylalkynyl, heteroarylalkynyl, substitutedheteroarylalkynyl, condensed polycyclic, substituted condensedpolycyclic, aryl, alkyl, heteroaryl, nitro, trifluoromethane, arylether, alkylether, heteroarylether, diarylamine, dialkylamine,diheteroarylamine, diarylborane, triarylsilane, trialkylsilane, alkenyl,alkylaryl, cycloalkyl, haloformyl, hydroxyl, aldehyde, carboxamide,amine, amino, alkoxy, azo, benzyl, carbonate ester, carboxylate,carboxyl, ketamine, isocyanate, isocyanide, isothiocyanate, nitrile,nitro, nitroso, phosphine, phosphate, phosphono, pyridyl, sulfonyl,sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted aryl, heteroaryl,substituted heteroaryl, heterocyclic, NRR′, SR, C(O)R, COOR, C(O)NR,SOR, SOR, BRR″ and derivatives thereof; and R and R′ are independentlyselected from the group consisting of hydrogen atom, deuterium atom,formaldehyde, cyano, alkylalkynyl, substituted alkylalkynyl,arylalkynyl, substituted arylalkynyl, heteroarylalkynyl, substitutedheteroarylalkynyl, condensed polycyclic, substituted condensedpolycyclic, aryl, alkyl, heteroaryl, nitro, trifluoromethane, cyano,arylether, alkylether, heteroarylether, diarylamine, dialkylamine,diheteroarylamine, diarylborane, triarylsilane, trialkylsilane, alkenyl,alkylaryl, cycloalkyl, haloformyl, hydroxyl, aldehyde, carboxamide,amine, amino, alkoxy, azo, benzyl, carbonate ester, carboxylate,carboxyl, ketamine, isocyanate, isocyanide, isothiocyanate, nitrile,nitro, nitroso, phosphine, phosphate, phosphono, pyridyl, sulfonyl,sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted aryl, heteroaryl,substituted heteroaryl, heterocyclic and derivatives thereof.

The term “aryl,” alone or in combination, includes carbocyclic aromaticsystems. The systems may contain one, two or three rings wherein eachring may be attached together in a pendant manner or may be fused. Forexample, the rings can be 5- or 6-membered rings. Aryl groups include,but not exclusive to, unsubstituted or substituted derivatives ofbenzene (phenyl), naphthylene, pyrene, anthracene, pentacene,benzo[a]pyrene, chrysene, coronene, corannulene, naphthacene,phenanthrene, triphenyklene, ovalene, benzophenanthrene, perylene,benzo[g,h,i]perylene, antanthrene, pentaphene, picene,dibenzo[3,4:9,10]pyrene, benzo[3,4]pyrene, dibenzo[3,4:8,9] pyrene,dibenzo[3,4;6,7]pyrene, dibenzo[1,2:3,4]pyrene, andnaphto[2,3;3,4]pyrene; wherein the positions of attachment andsubstitution can be at any carbon of the group that does not stericallyinhibit formation of compound of formula (I), as can be appreciated byone skilled in the art.

The term “heteroaryl,” alone or in combination, includes heterocyclicaromatic systems. The systems may contain one, two or three ringswherein each ring may be attached together in a pendant manner or may befused. For example, the rings can be 5- or 6-membered rings.Heterocyclic and heterocycle refer to a 3 to 7-membered ring containingat least one heteroatom. Heteroaryl groups include, but not exclusiveto, unsubstituted or substituted derivatives of pyridine, thiophene,furan, pyrazole, imidazole, oxazole, isoxazole, thiazole, isothiazole,pyrole, pyrazine, pyridazine, pyrimidine, benzimidazole, benzofuran,benzothiazole, benzopyrrolizinophenoxazine, indolocarbazole, oxadiazole,thiadiazole, indole, triazole, tetrazole, pyran, thiapyran, oxadiazole,triazine, tetrazine, carbazole, dibenzothiophene, dibenzofuran,isoindole, quinoline, isoquinoline, chromene, isochromene,thienopyridine, furopyridine, selenophenopyridine, and non-aromaticrings piperazine, piperidine, pyrolidine and thereof; wherein theposition of attachment or substitution can be at any carbon of the groupthat does not sterically inhibit formation of compound of formula (I),as can be appreciated by one skilled in the art.

The terms “heterocyclic” and “heterocycle” refer to a 3 to 7-memberednon-aromatic ring containing at least one heteroatom, and includespiperazine, piperidine, pyrrolidine, morpholine, thiomorpholine, pyran,thiopyran, dihydrofuranyl, tetrahydrofuranyl, dihydrothiophenyl,tetrahydrothiophenyl, dihydropyranyl, tetrahydropyranyl,dihydrothiazolyl and the like. The groups of the present disclosure canbe substituted or unsubstituted. Preferred substituents include but arenot limited to alkyl, alkoxy, aryl.

The term “heteroatom” as used herein includes S, O, N, P, Se, Te, As,Sb, Bi, B, Si, Ge, Sn and Pb.

The term “substituted” refers to any level of substitution althoughmono-, di- and tri-substitutions are preferred. Substituents includinghydrogen, halogen, aryl, alkyl, heteroaryl, nitro group,trifluoromethane group, cyano group, arylether, alkylether,heteroarylether, diarylamine, dialkylamine, diheteroarylamine,diarylborane, triarylsilane, trialkylsilane, alkenyl, alkylaryl,cycloalkyl, haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino,alkoxy, azo, benzyl, carbonate ester, carboxylate, carboxyl, ketamine,isocyanate, isocyanide, isothiocyanate, nitrile, nitro, nitroso,oxadiazole, thiadiazole, phosphine, phosphate, phosphono, pyridyl,sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted aryl,heteroaryl, substituted heteroaryl, heterocyclic group and thereof, thatare readily prepared.

Benzene includes substituted or unsubstituted benzene. Pyridine includessubstituted or unsubstituted pyridine. Thiophene includes substituted orunsubstituted thiophene. Furan includes substituted or unsubstitutedfuran. Pyrazole includes substituted or unsubstituted pyrazole.Imidazole includes substituted or unsubstituted imidazole. Oxazoleincludes substituted or unsubstituted oxazole. Isoxazole includessubstituted or unsubstituted isoxazole. Thiazole includes substituted orunsubstituted thiazole. Isothiazole includes substituted orunsubstituted isothiazole. Pyrrole includes substituted or unsubstitutedpyrole. Pyrazine includes substituted or unsubstituted pyrazine.Pyridazine includes substituted or unsubstituted pyridazine. Pyrimidineincludes substituted or unsubstituted pyrimidine. Benzimidazole includessubstituted or unsubstituted benzimidazole. Benzofuran includessubstituted or unsubstituted benzofuran. Benzothiazole includessubstituted or unsubstituted benzothiazole. Indole includes substitutedor unsubstituted indole. Naphthalene includes substituted orunsubstituted naphthalene. Triazole includes substituted orunsubstituted triazole. Tetrazole includes substituted or unsubstitutedtetrazole. Pyran includes substituted or unsubstitutedpyran. Thiapyranincludes substituted or unsubstituted thiapyran. Oxadiazole includessubstituted or unsubstituted oxadiazole. Triazine includes substitutedor unsubstituted triazine. Tetrazine includes substituted orunsubstituted tetrazine. Carbazole includes substituted or unsubstitutedcarbazole. Dibenzothiophene includes substituted or unsubstituteddibenzothiophene. Dibenzofuran includes substituted or unsubstituteddibenzofuran. Piperazine includes substituted or unsubstitutedpiperazine. Piperidine includes substituted or unsubstituted piperidine.Pyrrolidine includes substituted or unsubstituted pyrolidine.Indolocarbazole includes substituted or unsubstituted indolocarbazole.Benzopyrrolizinophenoxazine includes substituted or unsubstitutedbenzopyrrolizinophenoxazine. Thiadiazole includes substituted orunsubstituted thiadiazole.

5. DETAILED DESCRIPTION

Embodiments of the subject matter described herein are directed towardsthermally stable gold(III) compounds comprising highly rigidtetradentate ligands. Other embodiments of the subject matter describedherein are directed to modification of luminescent tetradentateligand-containing gold(III) compounds. The luminescent gold(III)compounds comprise a tetradentate ligand containing four ligating sitescoordinated to a gold(III) metal center. The ligation site consists ofcoordinating atoms that can be, for example, nitrogen, carbon, ora-donating groups, for example, aryl groups.

The luminescent tetradentate ligand-containing gold(III) compoundscomprise:

-   -   at least one gold metal center having a +3 oxidation state and        four coordination sites;    -   a tetradentate ligand bearing coordinating atoms or functional        groups as ligating site to coordinate to the gold center; and        the coordinating sites are connected directly or via an aromatic        system or spacer to form a rigid tetradentate ligand having four        coordination sites.

The luminescent gold(III) compounds of the present invention exhibithigh PLQY of 5-80% in solid-state thin films, and have been demonstratedto serve as phosphorescent dopants in the fabrication ofsolution-processable and vacuum-deposited OLEDs. The gold(III) compoundsdisclosed herein, when implemented in a high performancesolution-processable OLED, produce superior EL with high currentefficiencies of 10-80 cd A⁻¹, and high EQEs of 2-20%. This EQE valueimproves upon the values reported by other solution-processable OLEDsbased on gold(III) complexes. The compounds disclosed herein produceresults that are comparable to the state-of-the-art solution-processableOLEDs based on iridium(III) complexes and thermally activated delayedfluorescence (TADF) materials. In this way, the present inventionprovides new classes of phosphors for the OLED display and solid-statelighting industries that can be fabricated by using low-cost and highefficiency solution-processing techniques to obtainphosphorescence-based OLEDs.

The novel class of gold(III) compounds described herein further showseither strong photoluminescence via a triplet excited state uponphoto-excitation, or EL via a triplet exciton upon applying a DCvoltage. According to one or more embodiments herein, these gold(III)compounds are highly soluble in common organic solvents such asdichloromethane, chloroform and toluene. Alternatively, the compoundscan be doped into a host matrix for thin film deposition by spin-coatingor ink-jet printing or other known fabrication methods. In one or moreembodiments, the compounds can be used for the fabrication of OLEDs asphosphorescent emitters or dopants to generate EL.

While the gold(III) compounds described herein are described with use inOLEDs, the compounds have additional applications as would be understoodto those who are skilled in the art. The gold(III) compounds describedherein have strong light-emitting and light absorption properties thatmake them suitable for inclusion into common apparatuses for which lightemission or absorption are desired. For example, the gold(III) compoundsmay be used as, but not limited to, the backlighting of flat paneldisplays of wall-mounted televisions, copiers, printers, liquid crystaldisplays, measuring instruments, display boards, marker lamps,electrophotographic photoreceptors, photoelectric transducers, solarcells and image sensors.

The luminescent tetradentate ligand-containing gold(III) compounds havethe chemical structure shown in generic formula (I),

wherein:

-   -   (a) Z is selected from the group consisting of B, C, N, O, Si,        P, P(═O), S and Se;    -   (b) rings A and B are each coordinated to the Au atom through a        carbon atom, and are each independently a substituted or        unsubstituted aryl group, preferably a phenyl group, or a        substituted or unsubstituted heteroaryl group;    -   (c) ring C is coordinated to the Au atom through a nitrogen        atom, and is selected from the group consisting of a substituted        or unsubstituted pyridyl group, a substituted or unsubstituted        quinolinyl group, a substituted or unsubstituted isoquinolinyl        group, a substituted or unsubstituted pyrazinyl group, a        substituted or unsubstituted pyrimidinyl group, a substituted or        unsubstituted pyridazinyl group, a substituted or unsubstituted        triazinyl group, a substituted or unsubstituted carbolinyl        group, a substituted or unsubstituted imidazolyl group, a        substituted or unsubstituted benzimidazolyl group, a substituted        or unsubstituted pyrazolyl group, a substituted or unsubstituted        thienopyridinyl, a substituted or unsubstituted furopyridinyl        group, a substituted or unsubstituted selenophenopyridinyl        group, a substituted or unsubstituted thiazolyl group, a        substituted or unsubstituted thiadiazolyl group, a substituted        or unsubstituted oxadiazolyl group, a substituted or        unsubstituted triazolyl group, a substituted or unsubstituted        oxazolyl group and a substituted or unsubstituted isoxazolyl        group,    -   (d) each D is independently at each occurrence absent or a        cyclic or acyclic moiety wherein:        -   the cyclic moiety is selected from the group consisting of a            substituted or unsubstituted aryl group, preferably a phenyl            group, a substituted or unsubstituted heteroaryl group,            preferably a pyridyl group, a substituted or unsubstituted            cycloalkyl group, and a substituted or unsubstituted            polycyclic group; and        -   the acyclic moiety is selected from the group consisting of            a substituted or unsubstituted alkynyl, a substituted or            unsubstituted arylalkynyl, a substituted or unsubstituted            alkyl, a substituted or unsubstituted alkylaryl, a            substituted or unsubstituted alkoxy, a substituted or            unsubstituted arylalkoxy, a substituted or unsubstituted            acene, and a substituted or unsubstituted a heteroacene;    -   (e) E is absent, an acyclic moiety selected from the group        consisting of a substituted or unsubstituted alkynyl, a        substituted or unsubstituted arylalkynyl, a substituted or        unsubstituted alkyl, a substituted or unsubstituted alkylaryl, a        substituted or unsubstituted alkoxy, a substituted or        unsubstituted arylalkoxy, a substituted or unsubstituted        thiolate, a substituted or unsubstituted arylthiolate, a        substituted or unsubstituted phosphide, a substituted or        unsubstituted arylphosphide, a substituted or unsubstituted        boride, a substituted or unsubstituted arylboride, a substituted        or unsubstituted acene and a substituted or unsubstituted        heteroacene,        -   or E, together with Z and the atoms to which they are            respectfully attached forms a cyclic moiety selected from            the group consisting of a substituted or unsubstituted            pyridyl group, a substituted or unsubstituted pyrrolyl            group, a substituted or unsubstituted thiophenyl group, a            substituted or unsubstituted furanyl group, a substituted or            unsubstituted pyrazolyl group, a substituted or            unsubstituted oxazolyl group, a substituted or unsubstituted            imidazolyl group, a substituted or unsubstituted pyrazinyl            group, a substituted or unsubstituted pyrimidinyl group, a            substituted or unsubstituted pyridazinyl group, a            substituted or unsubstituted piperazinyl group, a            substituted or unsubstituted oxazinyl group, a substituted            or unsubstituted morpholinyl group, a substituted or            unsubstituted thiomorpholinyl group, a substituted or            unsubstituted thiazinyl group, and a substituted or            unsubstituted piperidinyl group;        -   or D, E and Z together represent a substituted or            unsubstituted, monocyclic or fused polycyclic aryl or            heteroaryl group;    -   (f) or D, Y and C, and/or D, Y and B, together represent a        substituted or unsubstituted, monocyclic or fused polycyclic        aryl or heteroaryl group;X and Y are each independently at each        occurrence non-coordination sites selected from the group        consisting of, —CRR′, —C═O, —NR, —O, —PR, —P(═O)R, —BR, S, —SO,        —SO₂, —SiRR′, Se, —AsR, —CH═CH— and —CR═CR—′, wherein R and R′        are independently selected from the group consisting of        hydrogen, halogen, aryl, alkyl, heteroaryl, nitro,        trifluoromethyl, cyano, arylether, alkylether, heteroaryl ether,        diarylamine, dialkylamine, diheteroarylamine, diarylborane,        triarylsilane, trialkylsiliane, alkenyl, alkylaryl, cycloalkyl,        haloformyl, hydroxyl, aldehyde, carboxamide, amine, amino,        alkoxy, azo, benzyl, carbonateester, carboxylate, carboxyl,        ketamine, isocyanate, isocyanide, isothiocyanate, nitrile,        nitro, nitroso, phosphine, phosphate, phosphono, pyridyl,        sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted        aryl, heteroaryl, substituted heteroaryl, a heterocyclic group        and derivatives thereof;    -   (g) wherein p, q, r and s are each independently 0, 1, 2 or 3;        and    -   (h) n is zero, a positive integer or a negative integer.

Specific examples of the luminescent tetradentate ligand-containinggold(III) compounds of formula (I) include the following:

In some embodiments of the subject matter described herein, theluminescent tetradentate ligand-containing gold(III) compounds offormula (I) are prepared. The compounds are represented throughout bytheir monomeric structure. As is well known to those skilled in the art,the compounds may also be present as dimers, trimers, oligomers ordendrimers.

The luminescent tetradentate ligand-containing gold(III) compounds canbe used to form thin films by spin-coating, vacuum deposition or otherknown fabrication methods and be applied in OLEDs. With reference now toFIG. 1, the gold(III) compounds as in one or more embodiments herein canbe fabricated into an OLED structure 100. The OLED structure 100includes a cathode 110, an electron transport layer 120 (“ETL”), alight-emitting layer 130 (or “emissive layer”), a hole-transportinglayer 140 (“HTL”), an anode 150, and a substrate 160. The light-emittinglayer 130 includes a luminescent gold(III) compound as described herein.Although not shown in FIG. 1, in one or more embodiments, OLED 100further includes a hole blocking layer and/or a carrier confinementlayer to improve the device performance. Device structures withmodifications to include various carrier blocking layers, carrierinjection layers and interlayers can also be used to improve the deviceperformance.

The cathode 110 and anode 150 are a pair of electrodes sandwiching theseplurality of semiconductor layers that cause EL when voltage is appliedto the OLED 100. The cathode 110 acts as a transmissive electroninjector that injects electrons into the organic emissive layer 130 whenthe cathode is negatively biased. The cathode comprises a thin fluoridelayer (which may be omitted) and a metal or metal alloy, preferablyhaving a work function of less than 4 eV. The cathode 110 may be made ofsuitable materials such as, for example, Mg:Ag, Ca, Li:Al, Al, or Ba.The anode 150 injects holes into the emissive layer when the anode ispositively biased. The anode 150 is composed of a conductive andoptionally transmissive layer. In one or more embodiments, viewing theemissive layer 130 through the substrate 160 is desirable, and the anodeis transparent. In other embodiments, the emissive layer 130 is viewedthrough the top electrode and the transmissive characteristics of anode150 are immaterial, and therefore any appropriate materials includingmetals or metal compounds having a work function of greater than 4.1 eVmay be used. For example, appropriate metals include silver, gold,iridium, nickel, molybdenum, palladium, and platinum. In one or moreembodiments, the anode 150 is transmissive, and suitable materials aremetal oxides, including indium-tin oxide, aluminum- or indium-doped zincoxide, tin oxide, magnesium-indium oxide, nickel-tungsten oxide, andcadmium-tin oxide. The preferred metals and metal oxides can bedeposited by evaporation, sputtering, laser ablation, and chemical vapordeposition. The cathode 110 and anode 150 can have thicknesses between100-200 nm.

In one or more embodiments, the anode 150 layer is positioned on top ofa substrate 160. The substrate 160 is electrically insulated and is usedto emit the light created by the OLED 100, in which it is typically madeof transparent material. For example, the substrate 160 can be made ofglass, plastic foil, or a transparent polymer. In one or morealternative embodiments, the substrate is opaque and comprises one ormore semiconducting materials or ceramics. In one embodiment of thesubject matter described herein, the emissive layer 130 is viewedthrough the substrate 160, or through both sides of the device, andsubstrate comprises a transparent glass substrate or a plastic foil. Inother embodiments, the emissive layer 130 is viewed only through the topelectrode, and substrate 160 comprises an opaque semiconductor orceramic wafers.

The ETL 120 provides high electron affinity and high electron mobilityto the OLED 100 for electrons to flow across the various OLED layers. Todo this, the electron-transporting layer 120 includes materials ormixtures of materials having a high ionization potential and wideoptical band gap. In one or more embodiments, the ETL 120 has athickness between 30-80 nm. In one or more embodiments, additionalelectron transporting materials are added to ETL 120 to facilitateelectron injection. The materials for the ETL 120 are selected tomaximize OLED efficiency. As some non-limiting examples, suitableelectron-transporting materials include but are not limited to1,3,5-tris(phenyl-2-benzimidazolyl)-benzene (TPB I),1,3,5-tri[(3-pyridyl)-phen-3-yl] benzene (TmPyPB), bathocuproine (BCP),bathophenanthroline (BPhen) andbis(2-methyl-8-quinolinolate)-4-(phenylphenolate)aluminum (BAlq),tris-[2,4,6-trimethyl-3-(pyridin-3-yl)phenyl]borane (3TPYMB), and1,3-bis [3,5-di(pyridin-3-yl)phenyl]benzene (BmPyPhB). In oneembodiment, the electron-transporting layer 120 is prepared as anorganic film by thermal evaporation, spin-coating, ink-jet printing froma solution, or other known fabrication methods. Light-emitting layer oremissive layer 130 in FIG. 1 is formed by doping the phosphorescentgold(III) metal complex as a dopant into a host material. Suitable hostmaterials should be selected so that the triplet excitons can betransferred efficiently from the host material to the phosphorescentdopant material. Suitable host materials include, but are not limitedto, certain aryl amines, triazoles and carbazole compounds. Examples ofdesirable hosts include, but are not limited to, CBP, MCP, TCTA,3-(4-biphenylyl)-4-phenyl-5-tert-butylphenyl-1,2,butylphenyl-1,2,4-triazole(TAZ), UGH2, and PVK. In certain embodiments, any one of the compounds 1to 220 can be doped into a mixed host consisting of non-limitingexamples of CBP, MCP, TCTA, TAZ, UGH2, PVK or a combination thereof.

In general, the emissive layer 130 is sandwiched between thehole-transporting layer 140 and the electron-transporting layer 120. Toensure an efficient exothermic energy transfer between the host materialand the dopant material, the triplet energy of the host material must belarger than that of the dopant material. In addition, both theionization potential and the electron affinity of the host materialshould be larger than those of the dopant material in order to achieveefficient Förster energy transfer from the host to the dopant. In orderto confine triplet excitons within the emissive layer, the tripletenergy of the hole-transporting material and electron-transportingmaterial should be larger than that of the dopant material.

The HTL 140 is layered on top of the anode 150 and plays a role in theadjustment of electron/hole injection to attain transport balance ofcharge carriers in the emissive layer 130 of the OLED 100. In one ormore embodiments, the HTL 140 has a thickness between 30-80 nm. Thematerials for the HTL 140 are selected to maximize OLED efficiency. Assome non-limiting examples, the HTL 140 can include, but is not limitedto, polycyclic aromatic compounds, for example,4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB),4,4′-bis[N-(3-methylphenyl)-N-phenylamino]biphenyl (TPD),4,4′,4″-tris[(3-methylphenyl)phenylamino] triphenylamine (MTDATA), anddi-[4-(N,N-ditolyl-amino)phenyl]cyclohexane (TAPC). In addition,polymeric hole-transporting materials can be used, including PVK,polythiophene, polypyrrole, polyaniline, and copolymers includingpoly(3,4-ethylenedioxythiophene):poly(styrene-sulfonate) (PEDOT:PSS).

In some embodiments of the subject matter described herein, luminescentgold(III) compounds are either the primary luminescent material or asecondary luminescent material in the device, as shown FIG. 1. In someembodiments of the subject matter described herein, the tetradentateligand-containing gold(III) compounds are employed aselectrophosphorescent dopants in multilayer OLED with an EQE of up to20.6%. Advantageously, the tetradentate ligand-containing gold(III)compounds can be deposited in the OLEDs by spin-coating, screenprinting, ink-jet printing and vacuum deposition. In addition, theincorporation of electron-transporting phosphine oxide moiety or itsanalogues helps to increase the overall device performance. The highsolubility of the luminescent tetradentate ligand-containing gold(III)compounds in a variety of organic solvents permits simple and economicmanufacturing and patterning of large-area displays.

In some embodiments of the subject matter described herein, theluminescent tetradentate ligand-containing gold(III) compounds offormula (I) are prepared in high purity. The synthetic method involvesproviding the luminescent tetradentate ligand-containing gold(III)compounds of formula (I) from the cyclometalated gold(III) precursorcompounds or their equivalents. The gold(III) precursor compounds can beprepared by any methods known to those skilled in the art, for example,but are not limited to, the methods disclosed in Kröhnke, F. Synthesis 1(1976); Wong, K. H.; Cheung, K. K.; Chan, M. C.; Che, C. M.Organometallics, 17, 5305 (1998); Yam, V W.-W.; Wong, K. M.-C.; Hung,L.-L.; Zhu, N. Angew. Chem. Int. Ed. 4, 3107 (205); Au, V.K.-M.; Wong,K.M.-C.; Zhu, N.; Yam, V W.-W. Chem. Eur. J. 17, 130 (2011); Roca,D.-A.; Smith, D. A.; Bochmann, M. Chem. Commun. 48, 7247 (2012); David,B.; Monkowius, U.; Rust, J.; Lehmann, C. W.; Hyzak, L.; Mohr, F. DaltonTrans. 43, 11059 (2014); Malty, A.; Sulicz, A. N.; Deligonul, N.; Zeler,M.; Hunter, A. D.; Gray, T. G. Chem. Sci. 6, 981 (2015); Kumar, R.;Linden, A.; Nevado, C. Angew. Chem. Int. Ed. 54, 14287 (2015).

In some parts of the subject matter described herein, the tetradentateligand-containing gold(III) compounds can be further modified byincorporation of the substituents to the tetradentate ligand-containinggold(III) compounds.

In some parts of the subject matter described herein, purification canbe carried out by any method or combination of methods, includingchromatography, extraction, crystallization, sublimation or anycombination thereof.

In one or more embodiments, the luminescent gold(III) compoundsdisclosed herein are deposited as a thin layer on a substrate layer. Inone or more embodiments, the thickness of the deposited gold(III)compound is 10-20 nm, 21-30 nm, 31-40 nm, 41-50 nm, 51-60 nm, 61-70 nm,71-80 nm, 81-90 nm, or 91-100 nm.

The present subject matter described herein will be illustrated morespecifically by the following non-limiting examples, it being understoodthat changes and variations can be made therein without deviating fromthe scope and the spirit of the disclosure as hereinafter claimed. It isalso understood that various theories as to why the disclosure works arenot intended to be limiting.

6. EXAMPLES

The following are examples that illustrate embodiments for practicingthe disclosure described herein. These examples should not be construedas limiting.

Example 1

Compounds 1-7 were prepared according to the following methodology asillustrated in Scheme 1. All the tetradentate ligand-containinggold(III) compounds were synthesized by the reaction of cyclometalatedgold(III) precursor compounds or their equivalents with thecorresponding heterocycles in the presence of a catalytic amount ofpalladium catalyst in base and organic solvent in one pot. For example,compound 1 was synthesized by stirring a mixture of [Au{C{circumflexover ( )}(4-C₆H₅)C{circumflex over ( )}NBr-6}Cl] (276 mg, 0.45 mmol)with3,6-di-tert-butyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(138 mg, 0.45 mmol), palladium catalyst and base in degassed solvent atreflux temperature overnight (Scheme 1). After removing the solvent, thecrude product was purified by dissolving in dichloromethane with slowdiffusion of diethyl ether. The solid was then filtered and dried undervacuum to give a yellow solid (102 mg). NMR spectra were recorded on aBruker AVANCE 500 or 600 (500 MHz, 600 MHz) Fourier-transform NMRspectrometer with chemical shifts reported relative to thetetramethylsilane (δ 0 ppm). The results of the analyses confirm thehigh purity of all the compounds.

-   -   wherein:

The characteristic spectroscopic properties of compounds 1-7 are asfollows:

Compound 1: Yield: 102 mg, 89%. ¹H NMR (500 MHz, CD₂Cl₂, 298 K, δ/ppm):δ 8.42 (s, 1H), 8.35 (d, J=8.5 Hz, 1H), 8.22 (s, 1H), 8.16 (s, 1H), 7.94(m, 1H), 7.85 (d, J=8.0 Hz, 1H), 7.80 (d, J=8.0 Hz, 1H), 7.66 (d, J=8.0Hz, 1H), 7.51-7.31 (m, 9H), 7.23-7.18 (m, 1H), 7.00 (t, J=7.5 Hz, 1H),1.53 (s, 18H). Positive ESI-MS: m/z 778.26 [M]⁺.

Compound 2: Yield: 76 mg, 68%. ¹H NMR (500 MHz, DMSO-d₆, 298 K, δ/ppm):δ 8.86 (d, J=8.5 Hz, 1H), 8.55 (d, J=8.0 Hz, 1H), 8.50-8.42 (m, 3H),8.29 (d, J=7.5 Hz, 1H), 8.20 (s, 1H), 7.98 (s, 1H), 7.91 (d, J=7.5 Hz,2H), 7.86 (d, J=8.0 Hz, 1H), 7.83-7.79 (m, 2H), 7.58-7.53 (m, 2H),7.48-7.35 (m, 3H), 7.30 (t, J=7.5 Hz, 1H), 7.22 (t, J=7.5 Hz, 1H), 7.07(t, J=7.5 Hz, 1H).

Compound 3: Yield: 54 mg, 77%. ¹H NMR (500 MHz, THF-d₈, 298 K, δ/ppm): δ8.65 (d, J=8.5 Hz, 1H), 8.37 (d, J=7.5 Hz, 1H), 8.30 (d, J=8.0 Hz, 1H),8.24-8.17 (m, 2H), 8.11 (d, J=7.5 Hz, 1H), 8.01-7.96 (m, 2H), 7.82 (s,1H), 7.68 (s, 1H), 7.64 (d, J=7.5 Hz, 2H), 7.52-7.47 (m, 3H), 7.36-7.31(m, 1H), 7.30-7.25 (m, 2H), 7.19-7.15 (m, 1H), 1.40 (s, 9H) 1.27 (s,9H).

Compound 4: Yield: 72 mg, 81%. ¹H NMR (500 MHz, THF-d₈, 298 K, δ/ppm): δ8.64 (d, J=8.0 Hz, 1H), 8.51 (d, J=1.6 Hz, 1H), 8.30 (s, 1H), 8.27 (d,J=1.6 Hz, 1H), 8.25-8.19 (m, 1H), 8.09 (d, J=8.0 Hz, 1H), 8.00 (d, J=1.6Hz, 1H), 7.89 (d, J=8.4 Hz, 1H), 7.84 (s, 1H), 7.70-7.62 (m, 3H),7.55-7.47 (m, 4H), 7.29 (dd, J=8.0 and 1.6 Hz, 1H), 1.62 (s, 9H), 1.54(s, 9H), 1.43 (s, 9H), 1.31 (s, 9H). Positive ESI-MS: m/z 890.38 [M]⁺.

Compound 5: Yield: 69 mg, 71%. ¹H NMR (500 MHz, CDCl₃, 298 K, δ/ppm): δ9.87 (s, 1H), 9.06 (s, 1H), 8.52 (s, 1H), 8.34 (s, 1H), 8.22 (s, 1H),8.04 (s, 1H), 7.99-7.97 (d, J=8.6 Hz, 1H), 7.69 (s, 1H), 7.61-7.58 (m,3H), 7.54-7.52 (d, J=8.2 Hz, 2H), 7.50-7.49 (d, J=8.0 Hz, 1H), 7.44-7.42(d, J=7.4 Hz, 1H), 7.31-7.29 (d, J=7.9 Hz, 1H), 1.59 (s, 9H), 1.50 (s,9H), 1.41 (s, 9H), 1.30 (s, 9H).

Compound 6: Yield: 32 mg, 59%. ¹H NMR (500 MHz, CDCl₃, 298 K, δ/ppm): δ8.73-8.70 (d, J=8.7 Hz, 1H), 8.37 (s, 1H), 8.29-8.27 (d, J=7.4 Hz, 1H),8.21-8.19 (d, J=7.6 Hz, 1H), 7.96 (s, 1H), 7.92-7.90 (d, J=7.7 Hz, 1H),7.84-7.82 (d, J=8.1 Hz, 1H), 7.79-7.77 (d, J=8.2 Hz, 1H), 7.72-7.68 (m,2H), 7.53-7.49 (m, 1H), 7.41-7.39 (m, 2H), 7.37-7.32 (m, 4H), 7.24-7.21(m, 4H), 1.40 (s, 9H), 1.20 (s, 9H).

Compound 7: Yield: 31 mg, 61%. ¹H NMR (500 MHz, Acetone-d₆, 298 K,δ/ppm): δ 9.37-9.35 (d, J=5.4 Hz, 1H), 8.43-8.41 (d, J=7.9 Hz, 1H),8.31-8.27 (m, 4H), 8.17 (s, 1H), 7.88-7.86 (d, J=11.1 Hz, 2H), 7.81-7.79(m, 2H), 7.68-7.66 (t, J=6.4 Hz, 1H), 7.45-7.43 (dd, J=8.5 and 1.5 Hz,1H), 1.56 (s, 9H), 1.51 (s, 9H), 1.47 (s, 9H), 1.47 (s, 9H).

Example 2

UV-Vis Absorption Properties

The UV-vis absorption spectra of compounds 1, 3 and 4 in toluenesolution at 298 K feature moderately intense vibronic-structuredabsorption bands at ca. 280-350 nm with extinction coefficients (ε) onthe order of 10⁴ dm³ mol⁻¹ cm⁻¹ (FIG. 2). These absorption bands aretentatively assigned as the intraligand (IL) [π→π*] transitions of thecyclometalating ligand and the carbazole moiety. On the other hand,broad and moderately intense structureless absorption bands at ca.410-530 nm have been observed for all the complexes. These absorptionbands are tentatively assigned as a mixture of metal-perturbed IL [π→π*]transitions of the cyclometalating ligands with some charge transfercharacter from the aryl ring to the pyridine unit and the IL chargetransfer (ILCT) [π(carbazole)→π*(pyridine)] transitions. Ametal-to-ligand charge transfer transition (MLCT) would not be likelydue to the non-reducing nature of the gold(III) center to achieve Au(IV)higher oxidation state. The UV-vis absorption data of compounds 1, 3 and4 in toluene solution at 298 K are summarized in TABLE 1.

TABLE 1 Photophysical data for compounds 1-4^([a]) Absorption λ_(max)/nmEmission Medium (ε_(max)/ λ_(max)/nm Compound (T/K) dm³mol⁻¹cm⁻¹)(τ_(o)/μs) Φ_(sol) ^([b]) Φ_(film) ^([c]) 1 Toluene (298) 318 (21590),554 (2.9) 0.07 0.66 379 (6590), 480 (15670) 2 — — 540  0.53^([d]) 3Toluene (298) 314 (21670), 528 (2.5) 0.04 0.55 345 (12500), 465 (14855)4 Toluene (298) 320 (18535), 549 (2.0) 0.05 0.49 343 (12645), 482(12640) ^([a])Compound 2 is only sparingly soluble in toluene at 298 K.^([b])The luminescence quantum yield, measured at room temperature using[Ru(bpy)₃Cl₂] in acetonitrile as the reference (excitation wavelength =436 nm, Φ_(lum) = 0.06). ^([c])Φ_(film) of gold(III) compound doped into10% MCP excited at wavelength of 320 nm. ^([d])Φ_(film) of gold(III)compound doped into 10% mCBP excited at wavelength of 320 nm.

Example 3

Emission Properties and Thermal Stabilities

Upon irradiation, compounds 1, 3 and 4 display luminescence at ca.528-554 nm with respectable PLQYs in both solution and solid-state thinfilms at room temperature (TABLE 1). The emission spectra of compounds1, 3 and 4 in degassed toluene solution are shown in FIG. 3. Uponexcitation at λ=436 nm in toluene solution at 298 K, broad structurelessemission bands have been observed for all complexes. These emissionbands are tentatively assigned as the ³ILCT [π(carbazole)→π*(pyridine)]transition. FIG. 4 shows the normalized emission spectra of thin filmsof compounds 1, 3, 4 and 7 doped in 10 wt % MCP at 298 K. The origins ofthese broad and structureless emission bands are tentatively assigned asthe ³ILCT [π(carbazole)→π*(pyridine)] transition, possibly with mixingof some excimeric emission. The assignments can be further supported bytheir emission energies upon varying the dopant concentrations in MCPthin films. The emission bands of compound 1 doped in 5 wt % to 20 wt %MCP at 298 K are found to be red-shifted with increasing dopantconcentration, which is characteristic of excimeric emission arisingfrom the π-π stacking of the cyclometalating tetradentate ligand (FIG. 5and TABLE 2). TGA have also be conducted for compounds 1-4. All of themexhibit high decomposition temperature (i.e. the temperature at whichthe material shows a 5% weight loss) of over 350 degree C. (FIGS. 6-9).

TABLE 2 Photophysical data for compound 1 doped in MCP thin film at 298K. Dopant Emission Concentration/wt % λ_(max)/nm Φ_(film) ^([a]) 5 5410.64 10 551 0.66 15 555 0.61 20 560 0.51 ^([a])Φ_(film) of gold(III)compound excited at wavelength of 320 nm.

Example 4

OLED Fabrication and Characterization

A solution-processable OLED according to an embodiment of the disclosurewas constructed in the following manner:

-   -   a) A transparent anode ITO-coated borosilicate glass substrate        (38 mm×38 mm) with sheet resistance of 30 Ω per square was        ultrasonicated in the commercial detergent Decon 90, rinsed in        deionized water having a resistivity of 18.2 Mega-ohm for 15        minutes, and then dried in an oven at 120 degree C. for an hour.        The substrate was next subjected to an UV-ozone treatment in a        Jelight 42-220 UVO-Cleaner equipped with a mercury grid lamp for        15 minutes in order to increase the work function of the        ITO-coated glass substrate for better hole injection into the        organic layer.    -   b) A 40-nm thick PEDOT:PSS hole-transporting layer was        spin-coated by using a Laurell WS-400Ez-6NPP-Lit2 single wafer        spin processor at 7000 rpm for 30 seconds onto the ITO-coated        glass substrate of step (a) and baked at 110 degree C. for 10        minutes in air.    -   c) A 30-nm thick light-emitting layer was spin-coated by using a        Laurell WS-400Ez-6NPP-Lit2 single wafer spin processor at 6000        rpm for 25 seconds onto PEDOT:PSS layer of step (b), and baked        at 80 degree C. for 10 minutes in air, in which compound 1 was        doped into light-emitting MCP layer at different concentrations        in the range from 5 to 20 wt %;    -   d) The substrate was put into a vacuum chamber, and the chamber        was pumped down from 1 bar to 5×10 mbar;    -   e) A 5-nm thick 3TPYMB hole blocking layer was deposited by        thermal evaporation on doped MCP light-emitting layer of step        (c).    -   f) A 30-nm TmPyPB electron-transporting layer was deposited by        thermal evaporation on the 3TPYMB layer of step (e).    -   g) A 0.8-nm thick LiF layer and a 80 nm thick Al layer were        deposited by thermal evaporation on the TmPyPB layer of step (f)        to form an electron-injecting cathode.

3TPYMB, TmPyPB, LiF and Al were prepared by thermal evaporation fromtantalum boats by applying current through the tantalum boats.Deposition rates were monitored with a quartz oscillation crystal and aSigma SQM-242 quartz crystal card and controlled at 0.1-0.2 nm s⁻¹ forboth organic and metal layers. Current density-voltage-luminancecharacteristics of organic EL devices were measured with a programmableKeithley model 2400 power source and a Spectrascan PR-655 colorimeterunder ambient air conditions.

As depicted in FIG. 10, the EL spectra for all the devices are almostidentical to their emission spectra in solution and solid-state thinfilms without any undesirable emission coming from the adjacentcarrier-transporting layers or the host materials. With increasing thedopant concentration, the peak maximum has been slightly red-shiftedfrom 544 nm to 556 nm, which is arising from the excimeric emissionarising from the π-π stacking of the cyclometalating tetradentateligand, in good agreement with the emission spectra of 1 in solid-statethin films. In addition, the optimized device doped with 15 wt %compound 1 demonstrates a high EQE of 6.7%, as shown in FIG. 11.

Example 5

The same materials and processing procedures were employed as describedin Example 4 except that compound 3 was doped into MCP as light emissivelayer. All the devices show a structureless green emission band withband maximum at 520 nm (FIG. 12). Notably, a smaller red shift of ˜290cm⁻¹ is observed, as compared to that for devices based on 1 (˜397cm⁻¹). Meanwhile, the optimized devices exhibit EQEs of up to 3.7% (FIG.13).

Example 6

The same materials and processing procedures were employed as describedin Example 4 except that compound 4 was doped into MCP as light emissivelayer. All the devices show a structureless green emission band withband maximum at 544 nm and the EL maximum remains almost unchanged uponincreasing the dopant concentration from 5 wt % to 20 wt % (FIG. 14).Meanwhile, the optimized devices exhibit EQEs of up to 7.4% (FIG. 15).

Example 7

A vacuum-deposited OLED according to an embodiment of the disclosure wasconstructed in the following manner:

-   -   a) A transparent anode ITO-coated borosilicate glass substrate        (38 mm×38 mm) with sheet resistance of 301 per square was        ultrasonicated in the commercial detergent Decon 90, rinsed in        deionized water having a resistivity of 18.2 Mega-ohm for 15        minutes, and then dried in an oven at 120 degree C. for an hour.        The substrate was next subjected to an UV-ozone treatment in a        Jelight 42-220 UVO-Cleaner equipped with a mercury grid lamp for        15 minutes in order to increase the work function of the        ITO-coated glass substrate for better hole injection into the        organic layer.    -   b) The substrate was put into a vacuum chamber, and the chamber        was pumped down from 1 bar to 5×10 mbar;    -   c) A 40-nm thick        N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)-2,2′-dimethylbenzidine        (α-NPD) hole-transporting layer was deposited by thermal        evaporation onto the ITO-coated glass substrate of step (a);    -   d) A 5-nm thick TCTA carrier confinement layer was deposited by        thermal evaporation onto the α-NPD of step (c);    -   e) A 20-nm thick light-emitting layer was deposited by thermal        evaporation onto the TCTA layer of step (d), in which 2, 5, 8,        11, and 14% compound 1 was doped into light-emitting        3,3′-di(9H-carbazol-9-yl)biphenyl (mCBP) layer;    -   f) A 50-nm thick        1,3,5-tris(6-(3-(pyridin-3-yl)phenyl)pyridine-2-yl)benzene        (Tm3PyP26PyB) electron-transporting layer was deposited by        thermal evaporation on doped mCBP light-emitting layer of step        (e).    -   g) A 1-nm thick LiF layer and a 150-nm thick Al layer were        deposited by thermal evaporation on the Tm3PyP26PyB layer of        step (f) to form an electron-injecting cathode.

All materials were prepared by thermal evaporation from tantalum boatsby applying current through the tantalum boats. Deposition rates weremonitored with a quartz oscillation crystal and a Sigma SQM-242 quartzcrystal card and controlled at 0.1-0.2 nm s⁻¹ for both organic and metallayers. Current density-voltage-luminance characteristics of organic ELdevices were measured with a programmable Keithley model 2400 powersource and a Spectrascan PR-655 colorimeter under ambient airconditions.

FIG. 14 depicts the EQEs of the vacuum-deposited devices based oncompound 1. Notably, high current efficiencies of 40.9 cd A⁻¹ and highEQEs of up to 13.1% can be realized for the optimized device doped with8 wt % compound 1 (FIG. 16).

Example 8

The same materials and processing procedures were employed as describedin Example 7 except that compound 2 was doped into mCBP as lightemissive layer. The optimized devices doped with 5 wt % compound 2exhibit high EQEs of 11.5% (FIG. 17).

Example 9

The same materials and processing procedures were employed as describedin Example 7 except that compound 3 was doped into mCBP as lightemissive layer. The optimized devices doped with 29 wt % compound 3exhibit high EQEs of 15.2% (FIG. 18).

Example 10

The same materials and processing procedures were employed as describedin Example 7 except that compound 4 was doped into mCBP as lightemissive layer. The optimized devices doped with 5 wt % compound 4exhibit high EQEs of 20.6% (FIG. 19).

Example 11

OLED Lifetime Measurement

A vacuum-deposited OLED according to an embodiment of the disclosure wasconstructed in the following manner:

-   -   a) A transparent anode ITO-coated borosilicate glass substrate        (38 mm×38 mm) with sheet resistance of 301 per square was        ultrasonicated in the commercial detergent Decon 90, rinsed in        deionized water having a resistivity of 18.2 Mega-ohm for 15        minutes, and then dried in an oven at 120 degree C. for an hour.        The substrate was next subjected to an UV-ozone treatment in a        Jelight 42-220 UVO-Cleaner equipped with a mercury grid lamp for        15 minutes in order to increase the work function of the        ITO-coated glass substrate for better hole injection into the        organic layer.    -   b) The substrate was put into a vacuum chamber, and the chamber        was pumped down from 1 bar to 5×10 mbar;    -   c) A 10-nm thick        dipyrazino[2,3-f:2′,3′-h]quinoxaline-2,3,6,7,10,11-hexacarbonitrile        (HATCN) hole-injection layer was deposited by thermal        evaporation onto the ITO-coated glass substrate of step (a);    -   d) A 40-nm thick α-NPD hole-transporting layer was deposited by        thermal evaporation onto the HATCN of step (c);    -   e) A 10-nm thick        9,9′,9″-triphenyl-9H,9′H,9″H-3,3′:6′,3″-tercarbazole (TrisPCz)        carrier confinement layer was deposited by thermal evaporation        onto the α-NPD of step (d);    -   f) A 40-nm thick light-emitting layer was deposited by thermal        evaporation onto the TrisPCz layer of step (e), in which 11%        compound 1 was doped into light-emitting        2,6-di(9H-carbazol-9-yl)pyridine (PYD-2Cz) layer;    -   g) A 10-nm thick        2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine (T2T)        hole-blocking layer was deposited by thermal evaporation onto        the doped PYD-2Cz layer of step (f);    -   h) A 40-nm thick 2,7-di(2,2′-bipyridin-5-yl)triphenylene        (BPyTP2) electron-transporting layer was deposited by thermal        evaporation on T2T layer of step (g);    -   i) A 1-nm thick LiF layer and a 150-nm thick Al layer were        deposited by thermal evaporation on the BPyTP2 layer of step (h)        to form an electron-injecting cathode.

All materials were prepared by thermal evaporation from tantalum boatsby applying current through the tantalum boats. Deposition rates weremonitored with a quartz oscillation crystal and a Sigma SQM-242 quartzcrystal card and controlled at 0.1-0.2 nm s⁻¹ for both organic and metallayers. Devices were encapsulated in a glovebox under nitrogen. Theoperational lifetime of the vacuum-deposited device was measured byMcScience OLED Lifetime Measurement System by accelerated lifetimetesting under a constant driving current density of 10 mA cm⁻² underambient conditions.

Example 12

The same materials and processing procedures were employed as describedin Example 10 except that compound 4 was doped into PYD-2Cz as lightemissive layer.

FIG. 20 depicts the relative luminance of devices as a function of time.Apparently, device based on compound 1 demonstrates a longer lifetime.Particularly, the estimated lifetime at LT₇₀ (i.e. the time required forthe luminance to drop to 70% of its initial value) of device based oncompound 1 is ˜11,060 hours and that for device based on compound 4 is˜5250 hours. In addition, the estimated half-lifetime of device based on1 is ˜29,740 hours. The shorter operational lifetime of device based oncompound 4 may be due to the formation of instable methyl radicals.

Throughout the specification, terms may have nuanced meanings suggestedor implied in context beyond an explicitly stated meaning. Likewise, thephrase “in one embodiment” as used herein does not necessarily refer tothe same embodiment and the phrase “in another embodiment” as usedherein does not necessarily refer to a different embodiment. Similarly,the phrase “one or more embodiments” as used herein does not necessarilyrefer to the same embodiment and the phrase “at least one embodiment” asused herein does not necessarily refer to a different embodiment. Theintention is, for example, that claimed subject matter includescombinations of example embodiments in whole or in part.

Example 13

The vacuum-deposited thin films of 11 v/v% 1, 3 and 4 doped in m-CBPhave been investigated by angular-dependent PL measurements. Theorientation order parameter (S) has been used to quantify the degree ofmolecular orientation, where S=0 is associated with a random molecularorientation and varies from S=−0.5 for perfect horizontal orientation toS=+1.0 for vertically-aligned molecules. FIG. 21 depicts the normalizedPL intensities as a function of the emission angle for the thin films,while FIG. 22 depicts the two-dimensional distribution of the emissionspectra vs the angle of the films, controlled by the automated rotatingstage. The incorporation of ^(t)Bu- groups onto the phenyl rings in 3and 4 yields negative values of S=−0.31 and S=−0.30, respectively, incontrast to the positive values of S=+0.10 in the absence of such^(t)Bu- groups in 1. This implies a preferential horizontal orientationof 3 and 4, and a slightly vertical orientation of 1 in the films. Giventhat 0 is the angle between the normal of a substrate and transitiondipole moment, S=−0.31, S=−0.30 and S=+0.10 correspond to the horizontaltransition dipole (Θ) of 0.87, 0.87 and 0.60, respectively. TABLE 3summarizes the molecular orientation parameters of 1, 3 and 4. It isworth noting that the Θ value of 0.87 represents one of the highestvalues in the reported literature among both the phosphorescent and TADFemitters, which also reinforces our molecular design that the restrictedrotation of the carbazolyl moiety in the tetradentate ligand would givea preferred molecular orientation. Thus, an understanding of thestructure-property relationship of this class of complexes would lead tothe identification of potential candidates with high 0 in thin films toimprove the out-coupling efficiency in OLEDs.

TABLE 3 Molecular orientation parameters of 1, 3 and 4 Complex OrderParameter (S) θ^(a)/° Θ^(b) (h:v)^(b) 1 +0.10 50.8 0.60 0.60:0.40 3−0.31 69.2 0.87 0.87:0.13 4 −0.30 68.6 0.87 0.87:0.13 ^(a)θ representsthe angle between the normal of a substrate and the transition dipolemoment vector and is calculated by the equation${S = {\frac{1}{2}{\langle{{3\cos^{2}\theta} - 1}\rangle}}},{{with}\mspace{14mu} {\langle\ldots\rangle}\mspace{14mu} {indicating}\mspace{14mu} {an}\mspace{14mu} {ensemble}\mspace{14mu} {{average}.}}$^(b)Θ represents the ratio of the horizontal dipole to the total dipoleof the emitters and is obtained by the equation Θ:(1−Θ) =<sin²θ>:<cos²θ> = h:v.

Example 14

Table 2 shows performance data of vacuum-deposited OLEDs based onCompounds 1, 2, and 4 measured at 1000 cd/m².

TABLE 2 Max. EQE (%) at Compound EQE (%) 1000 cd/m² 1 13.1 7.0 2 11.56.1 4 20.6 13.4 LT₇₀ (Hours) LT₅₀ (Hours) at Compound at 1000 cd/m² 1000cd/m² 1 221 593 4 105 189

TABLE 3 Compound 1 Compound 2 Compound 4 Type Dopant Dopant DopantDeposition process Vacuum- Vacuum- Vacuum- and weight % 8 wt % 5 wt % 8wt % CIE Color at 1,000 cd/m² 0.45, 0.54 0.32, 0.60 0.41, 0.57Efficiency roll-off 52 49 45 at 1,000 cd/m², % Decomposition 398 360 354temperature T_(d), ° C.

TABLE 4 CE [cd A⁻¹] ^(b) PE [lm W⁻¹] ^(c) EQE [%] ^(d) (maximum at at atBrightness) 1000 1000 1000 CIE Compound L [cd m⁻²]^(a) Max cd m⁻² Max cdm⁻² Max cd m⁻² [(x, y)] ^(e) 1 27,330 40.9 19.5 42.8 11.4 13.1 5.9 0.45,0.54 Vacuum-deposited 2 13,410 39.6 19.7 35.5 13.0 11.5 5.8 0.32, 0.60Vacuum-deposited 4 31,210 73.7 41.1 66.2 26.1 20.6 11.2 0.41, 0.57Vacuum-deposited

Example 15

Amount Breakdown for Synthesizing 1 g of Au(III) Complex 1

Table 5 shows chemicals used for the synthesis of 3.3 g precursorligand.

TABLE 5 Amount Chemicals Used Carbazole 2.0 g tert-butylchloride 4.9 mLAluminium chloride 4.8 g N-bromosuccinimide 1.8 g Bis(pinacolato)diboron5.6 g Bis(triphenylphosphine) 25 mg palladium(II) dichloride SodiumAcetate 2.7 g Dichloromethane 20 mL Toluene 50 mL 1,4-dioxane 50 mLSilica gel 1.25 kg

Table 6 shows chemicals used for the synthesis of 2.1 g Au(III)precursor complex.

TABLE 6 Amount Chemicals Used [1,1':3',1”-terphenyl]- 1.2 g 5'-ylboronicacid 2,6-dibromopyridine 1 g Mecuric acetate 1.4 g Gold(III) potassium1.3 g tetrachloride Acetonitrile 10 mL Dichloroethane 20 mL Silica gel1.25 kg

Table 7 shows chemicals used for the synthesis of 1 g Au(III) complex 1.

TABLE 7 Amount Chemicals Used Precursor ligand^([1]) 1.4 g Au(III)precursor complex^([2]) 2.1 g Bis(triphenylphosphine) 72 mgpalladium(II) dichloride Potassium carbonate 2.76 g Tetrahydrofuran 50mL Diethyl Ether 50 mL

The foregoing description of the specific embodiments will so fullyreveal the general nature of the disclosure that others can, by applyingknowledge within the skill of the relevant art(s) (including thecontents of the documents cited and incorporated by reference herein),readily modify and/or adapt for various applications such specificembodiments, without undue experimentation, without departing from thegeneral concept of the present disclosure. Such adaptations andmodifications are therefore intended to be within the meaning and rangeof equivalents of the disclosed embodiments, based on the teaching andguidance presented herein. It is to be understood that the phraseologyor terminology herein is for the purpose of description and not oflimitation, such that the terminology or phraseology of the presentspecification is to be interpreted by the skilled artisan in light ofthe teachings and guidance presented herein, in combination with theknowledge of one skilled in the relevant art(s).

While various embodiments of the present disclosure have been describedabove, it should be understood that they have been presented by way ofexamples, and not limitation. It would be apparent to one skilled in therelevant art(s) that various changes in form and detail could be madetherein without departing from the spirit and scope of the disclosure.Thus, the present disclosure should not be limited by any of theabove-described exemplary embodiments, but should be defined only inaccordance with the following claims and their equivalents.

What is claimed:
 1. A luminescent gold(III) compound having the chemicalstructure shown in the generic formula (I),

wherein: (a) Z is selected from the group consisting of B, C, N, O, Si,P, P(═O), S and Se; (b) rings A and B are each coordinated to the Auatom through a carbon atom, and are each independently a substituted orunsubstituted aryl group, preferably a phenyl group, or a substituted orunsubstituted heteroaryl group; (c) ring C is coordinated to the Au atomthrough a nitrogen atom, and is selected from the group consisting of asubstituted or unsubstituted pyridyl group, a substituted orunsubstituted quinolinyl group, a substituted or unsubstitutedisoquinolinyl group, a substituted or unsubstituted pyrazinyl group, asubstituted or unsubstituted pyrimidinyl group, a substituted orunsubstituted pyridazinyl group, a substituted or unsubstitutedtriazinyl group, a substituted or unsubstituted carbolinyl group, asubstituted or unsubstituted imidazolyl group, a substituted orunsubstituted benzimidazolyl group, a substituted or unsubstitutedpyrazolyl group, a substituted or unsubstituted thienopyridinyl, asubstituted or unsubstituted furopyridinyl group, a substituted orunsubstituted selenophenopyridinyl group, a substituted or unsubstitutedthiazolyl group, a substituted or unsubstituted thiadiazolyl group, asubstituted or unsubstituted oxadiazolyl group, a substituted orunsubstituted triazolyl group, a substituted or unsubstituted oxazolylgroup and a substituted or unsubstituted isoxazolyl group, (d) each D isindependently at each occurrence absent or a cyclic or acyclic moietywherein the cyclic moiety is selected from the group consisting of asubstituted or unsubstituted aryl group, preferably a phenyl group, asubstituted or unsubstituted heteroaryl group, preferably a pyridylgroup, a substituted or unsubstituted cycloalkyl group, and asubstituted or unsubstituted polycyclic group and the acyclic moiety isselected from the group consisting of a substituted or unsubstitutedalkynyl, a substituted or unsubstituted arylalkynyl, a substituted orunsubstituted alkyl, a substituted or unsubstituted alkylaryl, asubstituted or unsubstituted alkoxy, a substituted or unsubstitutedarylalkoxy, a substituted or unsubstituted acene, and a substituted orunsubstituted a heteroacene; (e) E is absent, an acyclic moiety selectedfrom the group consisting of a substituted or unsubstituted alkynyl, asubstituted or unsubstituted arylalkynyl, a substituted or unsubstitutedalkyl, a substituted or unsubstituted alkylaryl, a substituted orunsubstituted alkoxy, a substituted or unsubstituted arylalkoxy, asubstituted or unsubstituted thiolate, a substituted or unsubstitutedarylthiolate, a substituted or unsubstituted phosphide, a substituted orunsubstituted arylphosphide, a substituted or unsubstituted boride, asubstituted or unsubstituted arylboride, a substituted or unsubstitutedacene; and a substituted or unsubstituted heteroacene, or E, togetherwith Z and the atoms to which they are respectfully attached forms acyclic moiety selected from the group consisting of a substituted orunsubstituted pyridyl group, a substituted or unsubstituted pyrrolylgroup, a substituted or unsubstituted thiophenyl group, a substituted orunsubstituted furanyl group, a substituted or unsubstituted pyrazolylgroup, a substituted or unsubstituted oxazolyl group, a substituted orunsubstituted imidazolyl group, a substituted or unsubstituted pyrazinylgroup, a substituted or unsubstituted pyrimidinyl group, a substitutedor unsubstituted pyridazinyl group, a substituted or unsubstitutedpiperazinyl group, a substituted or unsubstituted oxazinyl group, asubstituted or unsubstituted morpholinyl group, a substituted orunsubstituted thiomorpholinyl group, a substituted or unsubstitutedthiazinyl group, and a substituted or unsubstituted piperidinyl group;or D, E and Z together represent a substituted or unsubstituted,monocyclic or fused polycyclic aryl or heteroaryl group; or D, Y and C,and/or D, Y and B, together represent a substituted or unsubstituted,monocyclic or fused polycyclic aryl or heteroaryl group; (f) X and Y areeach independently at each occurrence non-coordination sites selectedfrom the group consisting of, —CRR′, —C═O, —NR, —O, —PR, —P(═O)R, —BR,S, —SO, —SO₂, —SiRR′, Se, —AsR, —CH═CH— and —CR═CR—′, wherein R and R′are independently selected from the group consisting of hydrogen,halogen, aryl, alkyl, heteroaryl, nitro, trifluoromethyl, cyano,arylether, alkylether, heteroaryl ether, diarylamine, dialkylamine,diheteroarylamine, diarylborane, triarylsilane, trialkylsiliane,alkenyl, alkylaryl, cycloalkyl, haloformyl, hydroxyl, aldehyde,carboxamide, amine, amino, alkoxy, azo, benzyl, carbonateester,carboxylate, carboxyl, ketamine, isocyanate, isocyanide, isothiocyanate,nitrile, nitro, nitroso, phosphine, phosphate, phosphono, pyridyl,sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted aryl,heteroaryl, substituted heteroaryl, a heterocyclic group and derivativesthereof; (g) wherein p, q, r and s are each independently 0, 1, 2 or 3;and (h) n is zero, a positive integer or a negative integer.
 2. Thegold(III) compound according to claim 1, wherein the compound isdeposited as a thin layer on a substrate layer.
 3. The gold(III)compound according to claim 2, wherein the thin layer is prepared byvacuum deposition, spin-coating, or inkjet printing.
 4. The gold(III)compound according to claim 1, wherein the compound hasphotoluminescence properties within a range of about 380 to 1050 nm. 5.The gold(III) compound according to claim 1, wherein the compound emitslight in response to the passage of an electric current or to a strongelectric field.
 6. The gold(III) compound according to claim 1, whereinthe compound is used to fabricate an OLED.
 7. The gold(III) compoundaccording to claim 6, wherein the gold(III) compound serves as thelight-emitting layer of the OLED.
 8. The gold(III) compound according toclaim 7, wherein the gold(III) compound serves as a dopant in thelight-emitting layer or emissive layer of the OLED.
 9. A gold(III)compound having one of the following structures:


10. A method for preparing a luminescent compound with cyclometalatedtetradentate ligand comprising the step of:

wherein: (a) G and K are different from each other and independentlyselected from the group consisting of C and N; (b) R¹, R², R³, R⁴ and R⁵groups are each independently selected from the group consisting of OR,NR₂, SR, C(O)R, C(O)OR, C(O)NR₂, CN, CF₃, NO₂, SO₂, SOR, SO₂R, SO₃R,halo alkyl, alkenyl, alkynyl, alkylaryl, aryl and cycloalkyl wherein oneor more alkyl, alkenyl, alkynyl, alkylaryl, aryl or cycloalkyl isoptionally substituted with one or more OR, NR₂, SR, C(O)R, C(O)OR,C(O)NR₂, CN, CF₃, NO₂, SO₂, SOR, SO₂R, SO₃R, halo, aryl, substitutedaryl, heteroaryl, substituted heteroaryl or a heterocyclic group,wherein R is independently at each occurrence alkyl, alkynyl, alkylaryl,aryl or cycloalkyl; and (c) n is zero, a positive integer or a negativeinteger.
 11. The method according to claim 10, wherein the gold(III)metal center comprises a light-emitting layer of a light-emittingdevice.
 12. The method according to claim 10, wherein the gold(III)metal group comprises a layer of a light-emitting device.
 13. Thegold(III) compound according to claim 10, wherein the gold(III) metalcompound is a dopant included in the light-emitting layer or emissivelayer of the light-emitting device.
 14. The method according to claim10, wherein the gold(III) metal compound is a dopant included in alight-emitting device.
 15. A light-emitting device with an orderedstructure comprising an anode, a hole-transporting layer, alight-emitting layer, an electron-transporting layer and a cathodewherein the light-emitting layer comprises a gold(III) compound having achemical structure represented by the following general formula (I),

wherein: (a) Z is selected from the group consisting of B, C, N, O, Si,P, P(═O), S and Se; (b) rings A and B are each coordinated to the Auatom through a carbon atom, and are each independently a substituted orunsubstituted aryl group, preferably a phenyl group, or a substituted orunsubstituted heteroaryl group; (c) ring C is coordinated to the Au atomthrough a nitrogen atom, and is selected from the group consisting of asubstituted or unsubstituted pyridyl group, a substituted orunsubstituted quinolinyl group, a substituted or unsubstitutedisoquinolinyl group, a substituted or unsubstituted pyrazinyl group, asubstituted or unsubstituted pyrimidinyl group, a substituted orunsubstituted pyridazinyl group, a substituted or unsubstitutedtriazinyl group, a substituted or unsubstituted carbolinyl group, asubstituted or unsubstituted imidazolyl group, a substituted orunsubstituted benzimidazolyl group, a substituted or unsubstitutedpyrazolyl group, a substituted or unsubstituted thienopyridinyl, asubstituted or unsubstituted furopyridinyl group, a substituted orunsubstituted selenophenopyridinyl group, a substituted or unsubstitutedthiazolyl group, a substituted or unsubstituted thiadiazolyl group, asubstituted or unsubstituted oxadiazolyl group, a substituted orunsubstituted triazolyl group, a substituted or unsubstituted oxazolylgroup and a substituted or unsubstituted isoxazolyl group, (d) each D isindependently at each occurrence absent or a cyclic or acyclic moietywherein: the cyclic moiety is selected from the group consisting of asubstituted or unsubstituted aryl group, preferably a phenyl group, asubstituted or unsubstituted heteroaryl group, preferably a pyridylgroup, a substituted or unsubstituted cycloalkyl group, and asubstituted or unsubstituted polycyclic group; and the acyclic moiety isselected from the group consisting of a substituted or unsubstitutedalkynyl, a substituted or unsubstituted arylalkynyl, a substituted orunsubstituted alkyl, a substituted or unsubstituted alkylaryl, asubstituted or unsubstituted alkoxy, a substituted or unsubstitutedarylalkoxy, a substituted or unsubstituted acene, and a substituted orunsubstituted a heteroacene; (e) E is absent, an acyclic moiety selectedfrom the group consisting of a substituted or unsubstituted alkynyl, asubstituted or unsubstituted arylalkynyl, a substituted or unsubstitutedalkyl, a substituted or unsubstituted alkylaryl, a substituted orunsubstituted alkoxy, a substituted or unsubstituted arylalkoxy, asubstituted or unsubstituted thiolate, a substituted or unsubstitutedarylthiolate, a substituted or unsubstituted phosphide, a substituted orunsubstituted arylphosphide, a substituted or unsubstituted boride, asubstituted or unsubstituted arylboride, a substituted or unsubstitutedacene and a substituted or unsubstituted heteroacene, or E, togetherwith Z and the atoms to which they are respectfully attached forms acyclic moiety selected from the group consisting of a substituted orunsubstituted pyridyl group, a substituted or unsubstituted pyrrolylgroup, a substituted or unsubstituted thiophenyl group, a substituted orunsubstituted furanyl group, a substituted or unsubstituted pyrazolylgroup, a substituted or unsubstituted oxazolyl group, a substituted orunsubstituted imidazolyl group, a substituted or unsubstituted pyrazinylgroup, a substituted or unsubstituted pyrimidinyl group, a substitutedor unsubstituted pyridazinyl group, a substituted or unsubstitutedpiperazinyl group, a substituted or unsubstituted oxazinyl group, asubstituted or unsubstituted morpholinyl group, a substituted orunsubstituted thiomorpholinyl group, a substituted or unsubstitutedthiazinyl group, and a substituted or unsubstituted piperidinyl group;or D, E and Z together represent a substituted or unsubstituted,monocyclic or fused polycyclic aryl or heteroaryl group; or D, Y and C,and/or D, Y and B, together represent a substituted or unsubstituted,monocyclic or fused polycyclic aryl or heteroaryl group; (f) X and Y areeach independently at each occurrence non-coordination sites selectedfrom the group consisting of, —CRR′, —C═O, —NR, —O, —PR, —P(═O)R, —BR,S, —SO, —SO₂, —SiRR′, Se, —AsR, —CH═CH— and —CR═CR—′, wherein R and R′are independently selected from the group consisting of hydrogen,halogen, aryl, alkyl, heteroaryl, nitro, trifluoromethyl, cyano,arylether, alkylether, heteroaryl ether, diarylamine, dialkylamine,diheteroarylamine, diarylborane, triarylsilane, trialkylsiliane,alkenyl, alkylaryl, cycloalkyl, haloformyl, hydroxyl, aldehyde,carboxamide, amine, amino, alkoxy, azo, benzyl, carbonateester,carboxylate, carboxyl, ketamine, isocyanate, isocyanide, isothiocyanate,nitrile, nitro, nitroso, phosphine, phosphate, phosphono, pyridyl,sulfonyl, sulfo, sulfinyl, sulfhydryl, halo, aryl, substituted aryl,heteroaryl, substituted heteroaryl, a heterocyclic group and derivativesthereof; (g) wherein p, q, r and s are each independently 0, 1, 2 or 3;and (h) n is zero, a positive integer or a negative integer.
 16. Thelight-emitting device of claim 16, wherein the light-emitting layer oremissive layer is prepared using vacuum deposition or solutionprocessing technique.
 17. An apparatus comprising: a compound of claim1, and wherein the apparatus is selected from the group consisting of atelevision, a copier, a printer, a liquid crystal display, a measuringinstrument, a display board, a marker lamp, an electrophotographicphotoreceptor, a photoelectric transducer, a solar cell or an imagesensor, such that the apparatus incorporates the compound for lightemission purposes.